The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
126233953 12623395 3 F 20160921 20160804 20160927 PER US-ACTELION-A-NJ2016-139825 ACTELION 77.00 YR E F Y 0.00000 20160927 OT US US

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
126233953 12623395 1 PS VENTAVIS ILOPROST 1 Respiratory (inhalation) U U 21779 INHALATION VAPOUR, SOLUTION
126233953 12623395 2 SS AMBRISENTAN AMBRISENTAN 1 Unknown 5 MG, QD 1413180A 0 5 MG QD
126233953 12623395 3 C REVATIO SILDENAFIL CITRATE 1 U 0
126233953 12623395 4 C TREPROSTINIL DIOLAMIN TREPROSTINIL DIOLAMINE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126233953 12623395 1 Pulmonary arterial hypertension
126233953 12623395 2 Pulmonary arterial hypertension

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126233953 12623395 Bladder disorder
126233953 12623395 Cough
126233953 12623395 Dyspnoea
126233953 12623395 Nasopharyngitis
126233953 12623395 Oropharyngeal pain
126233953 12623395 Unevaluable event

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
126233953 12623395 2 20110816 0